ENST00000225964.10:c.4364G>A
MANE Select
|
ENSP00000225964.6:p.Gly1455Asp
|
|
ENST00000225964.9:c.4364G>A
|
ENSP00000225964.5:p.Gly1455Asp
|
|
NM_000088.3:c.4364G>A , LRG_1t1:c.4364G>A
|
NP_000079.2:p.Gly1455Asp
|
|
XM_005257058.3:c.4094G>A
|
XP_005257115.2:p.Gly1365Asp
|
|
XM_005257059.3:c.3446G>A
|
XP_005257116.2:p.Gly1149Asp
|
|
XM_011524341.1:c.4166G>A
|
XP_011522643.1:p.Gly1389Asp
|
|
XM_005257058.4:c.4094G>A
|
XP_005257115.2:p.Gly1365Asp
|
|
XM_005257059.4:c.3446G>A
|
XP_005257116.2:p.Gly1149Asp
|
|
NM_000088.4:c.4364G>A
MANE Select
|
NP_000079.2:p.Gly1455Asp
|
|